Found: 9
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Investigation of Epistasis Between the Serotonin Transporter and Norepinephrine Transporter Genes in Anorexia Nervosa.
- Published in:
- Neuropsychopharmacology, 2003, v. 28, n. 7, p. 1351, doi. 10.1038/sj.npp.1300204
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- Publication type:
- Article
STRUCTURE OF HUMAN RENIN AND EXPRESSION OF THE RENIN GENE.
- Published in:
- Clinical & Experimental Pharmacology & Physiology, 1984, v. 11, n. 4, p. 369, doi. 10.1111/j.1440-1681.1984.tb00281.x
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- Publication type:
- Article
An investigation of NOS2A promoter polymorphisms in Australian multiple sclerosis patients.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 7, p. 815, doi. 10.1038/sj.ejhg.5201422
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- Publication type:
- Article
Gene-gene interaction between the monoamine oxidase A gene and solute carrier family 6 (neurotransmitter transporter, noradrenalin) member 2 gene in anorexia nervosa (restrictive subtype).
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 12, p. 945, doi. 10.1038/sj.ejhg.5201077
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- Publication type:
- Article
Identification of 11 novel and common single nucleotide polymorphisms in the interleukin-7 receptor-a gene and their associations with multiple sclerosis.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 7, p. 509, doi. 10.1038/sj.ejhg.5200994
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- Publication type:
- Article
Fracture during Intravenous Bisphosphonate Treatment in a Child with Osteogenesis Imperfecta: An Argument for a More Frequent, Low-Dose Treatment Regimen.
- Published in:
- Hormone Research in Paediatrics, 2014, v. 81, n. 3, p. 204, doi. 10.1159/000355111
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- Publication type:
- Article
Fatal late-onset ornithine transcarbamylase deficiency after coronary artery bypass surgery.
- Published in:
- 2007
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- Publication type:
- journal article
The Australian Reproductive Genetic Carrier Screening Project (Mackenzie's Mission): Design and Implementation.
- Published in:
- Journal of Personalized Medicine, 2022, v. 12, n. 11, p. 1781, doi. 10.3390/jpm12111781
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- Publication type:
- Article
Paternal retraction of a fragile X allele to normal size, showing normal function over two generations.
- Published in:
- American Journal of Medical Genetics. Part A, 2022, v. 188, n. 1, p. 304, doi. 10.1002/ajmg.a.62500
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- Publication type:
- Article